Tracking Resilience to Infections by Mapping Disease Space.

Infected hosts differ in their responses to pathogens; some hosts are resilient and recover their original health, whereas others follow a divergent path and die. To quantitate these differences, we propose mapping the routes infected individuals take through "disease space." We find that...

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Main Authors: Brenda Y Torres, Jose Henrique M Oliveira, Ann Thomas Tate, Poonam Rath, Katherine Cumnock, David S Schneider
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-04-01
Series:PLoS Biology
Online Access:http://europepmc.org/articles/PMC4835107?pdf=render
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spelling doaj-416477899d5241109ed8810b2d51ded32021-07-02T06:05:43ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852016-04-01144e100243610.1371/journal.pbio.1002436Tracking Resilience to Infections by Mapping Disease Space.Brenda Y TorresJose Henrique M OliveiraAnn Thomas TatePoonam RathKatherine CumnockDavid S SchneiderInfected hosts differ in their responses to pathogens; some hosts are resilient and recover their original health, whereas others follow a divergent path and die. To quantitate these differences, we propose mapping the routes infected individuals take through "disease space." We find that when plotting physiological parameters against each other, many pairs have hysteretic relationships that identify the current location of the host and predict the future route of the infection. These maps can readily be constructed from experimental longitudinal data, and we provide two methods to generate the maps from the cross-sectional data that is commonly gathered in field trials. We hypothesize that resilient hosts tend to take small loops through disease space, whereas nonresilient individuals take large loops. We support this hypothesis with experimental data in mice infected with Plasmodium chabaudi, finding that dying mice trace a large arc in red blood cells (RBCs) by reticulocyte space as compared to surviving mice. We find that human malaria patients who are heterozygous for sickle cell hemoglobin occupy a small area of RBCs by reticulocyte space, suggesting this approach can be used to distinguish resilience in human populations. This technique should be broadly useful in describing the in-host dynamics of infections in both model hosts and patients at both population and individual levels.http://europepmc.org/articles/PMC4835107?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Brenda Y Torres
Jose Henrique M Oliveira
Ann Thomas Tate
Poonam Rath
Katherine Cumnock
David S Schneider
spellingShingle Brenda Y Torres
Jose Henrique M Oliveira
Ann Thomas Tate
Poonam Rath
Katherine Cumnock
David S Schneider
Tracking Resilience to Infections by Mapping Disease Space.
PLoS Biology
author_facet Brenda Y Torres
Jose Henrique M Oliveira
Ann Thomas Tate
Poonam Rath
Katherine Cumnock
David S Schneider
author_sort Brenda Y Torres
title Tracking Resilience to Infections by Mapping Disease Space.
title_short Tracking Resilience to Infections by Mapping Disease Space.
title_full Tracking Resilience to Infections by Mapping Disease Space.
title_fullStr Tracking Resilience to Infections by Mapping Disease Space.
title_full_unstemmed Tracking Resilience to Infections by Mapping Disease Space.
title_sort tracking resilience to infections by mapping disease space.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2016-04-01
description Infected hosts differ in their responses to pathogens; some hosts are resilient and recover their original health, whereas others follow a divergent path and die. To quantitate these differences, we propose mapping the routes infected individuals take through "disease space." We find that when plotting physiological parameters against each other, many pairs have hysteretic relationships that identify the current location of the host and predict the future route of the infection. These maps can readily be constructed from experimental longitudinal data, and we provide two methods to generate the maps from the cross-sectional data that is commonly gathered in field trials. We hypothesize that resilient hosts tend to take small loops through disease space, whereas nonresilient individuals take large loops. We support this hypothesis with experimental data in mice infected with Plasmodium chabaudi, finding that dying mice trace a large arc in red blood cells (RBCs) by reticulocyte space as compared to surviving mice. We find that human malaria patients who are heterozygous for sickle cell hemoglobin occupy a small area of RBCs by reticulocyte space, suggesting this approach can be used to distinguish resilience in human populations. This technique should be broadly useful in describing the in-host dynamics of infections in both model hosts and patients at both population and individual levels.
url http://europepmc.org/articles/PMC4835107?pdf=render
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